Publications of Matthias Lienhard
All genres
Journal Article (36)
Journal Article
10 (1), 10:55 (2018)
Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistance. Genome Medicine
Journal Article
11 (10), pp. 1889 - 1907 (2016)
Analyzing and interpreting genome data at the network level with ConsensusPathDB. Nature Protocols
Journal Article
48 (6), pp. 593 - 599 (2016)
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nature Genetics
Journal Article
526 (7571), pp. 68 - 74 (2015)
A global reference for human genetic variation. Nature
Journal Article
112 (31), pp. E4236 - E4245 (2015)
Simultaneous deletion of the methylcytosine oxidases Tet1 and Tet3 increases transcriptome variability in early embryogenesis. Proceedings of the National Academy of Sciences of the United States of America
Journal Article
17 (5), pp. 545 - 557 (2015)
The histone deacetylase SIRT6 controls embryonic stem cell fate via TET-mediated production of 5-hydroxymethylcytosine. Nature Cell Biology
Journal Article
42 (14), e110 (2014)
ARH-seq: identification of differential splicing in RNA-seq data. Nucleic Acids Research (London)
Journal Article
15 (8), pp. 777 - 788 (2014)
Epigenomic analysis of primary human T cells reveals enhancers associated with TH2 memory cell differentiation and asthma susceptibility. Nature Immunology
Journal Article
5, 5:3934 (2014)
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. Nature Communications
Journal Article
30 (2), pp. 284 - 286 (2014)
MEDIPS: genome-wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics
Journal Article
30 (2), pp. 284 - 286 (2014)
MEDIPS: genome wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics
Journal Article
30 (2), pp. 284 - 286 (2014)
MEDIPS: genome-wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics
Journal Article
342 (6154), p. 1235587 - 1235587 (2013)
Integrative annotation of variants from 1092 humans: application to cancer genomics. Science
Journal Article
9 (2), p. e1003250 - e1003250 (2013)
DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer. PLoS Genetics
Journal Article
130 (2), pp. 427 - 439 (2012)
RNA-Seq provides new insights in the transcriptome responses induced by the carcinogen benzo[a]pyrene. Toxicological Sciences
Journal Article
491 (7422), pp. 56 - 65 (2012)
An integrated map of genetic variation from 1,092 human genomes. Nature Book Chapter (1)
Book Chapter
Quantitative Comparison of Large-Scale DNA Enrichment Sequencing Data. In: Statistical Genomics (Eds. Mathé, E.; Davis, S.) (2016)
Thesis - PhD (1)
Thesis - PhD
Computational Analysis of Genome-wide Methylation Enrichment Experiments. Dissertation, xii, 125 pp. (2017)
Thesis - Master (1)
Thesis - Master
Analysis of RNA-seq experiments. Master, Freie Universität, Berlin (2011)